Zheng Z - Search Results

1

QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.

Zheng Z, Huang D, Wang J, Zhao K, Zhou Y, Guo Z, Zhai S, Xu H, Cui H, Yao H, Wang Z, Yi X, Zhang S, Sham PC, Li MJ. Zheng Z, et al. Nucleic Acids Res. 2020 Jan 8;48(D1):D983-D991. doi: 10.1093/nar/gkz888. Nucleic Acids Res. 2020. PMID: 31598699 Free PMC article.

2

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.

Huang D, Yi X, Zhang S, Zheng Z, Wang P, Xuan C, Sham PC, Wang J, Li MJ. Huang D, et al. Among authors: zheng z. Nucleic Acids Res. 2018 Jul 2;46(W1):W114-W120. doi: 10.1093/nar/gky407. Nucleic Acids Res. 2018. PMID: 29771388 Free PMC article.

3

Activation of P-TEFb by cAMP-PKA signaling in autosomal dominant polycystic kidney disease.

Sun Y, Liu Z, Cao X, Lu Y, Mi Z, He C, Liu J, Zheng Z, Li MJ, Li T, Xu D, Wu M, Cao Y, Li Y, Yang B, Mei C, Zhang L, Chen Y. Sun Y, et al. Among authors: zheng z. Sci Adv. 2019 Jun 5;5(6):eaaw3593. doi: 10.1126/sciadv.aaw3593. eCollection 2019 Jun. Sci Adv. 2019. PMID: 31183407 Free PMC article.

4

CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.

Wang J, Huang D, Zhou Y, Yao H, Liu H, Zhai S, Wu C, Zheng Z, Zhao K, Wang Z, Yi X, Zhang S, Liu X, Liu Z, Chen K, Yu Y, Sham PC, Li MJ. Wang J, et al. Among authors: zheng z. Nucleic Acids Res. 2020 Jan 8;48(D1):D807-D816. doi: 10.1093/nar/gkz1026. Nucleic Acids Res. 2020. PMID: 31691819 Free PMC article.

5

The support of genetic evidence for cardiovascular risk induced by antineoplastic drugs.

Cui H, Zuo S, Liu Z, Liu H, Wang J, You T, Zheng Z, Zhou Y, Qian X, Yao H, Xie L, Liu T, Sham PC, Yu Y, Li MJ. Cui H, et al. Among authors: zheng z. Sci Adv. 2020 Oct 14;6(42):eabb8543. doi: 10.1126/sciadv.abb8543. Print 2020 Oct. Sci Adv. 2020. PMID: 33055159 Free PMC article.

6

Cell-Type-Specific Gene Modules Related to the Regional Homogeneity of Spontaneous Brain Activity and Their Associations With Common Brain Disorders.

Shen J, Yang B, Xie Z, Wu H, Zheng Z, Wang J, Wang P, Zhang P, Li W, Ye Z, Yu C. Shen J, et al. Among authors: zheng z. Front Neurosci. 2021 Apr 20;15:639527. doi: 10.3389/fnins.2021.639527. eCollection 2021. Front Neurosci. 2021. PMID: 33958982 Free PMC article.

7

Interrogating cell type-specific cooperation of transcriptional regulators in 3D chromatin.

Yi X, Zheng Z, Xu H, Zhou Y, Huang D, Wang J, Feng X, Zhao K, Fan X, Zhang S, Dong X, Wang Z, Shen Y, Cheng H, Shi L, Li MJ. Yi X, et al. Among authors: zheng z. iScience. 2021 Nov 18;24(12):103468. doi: 10.1016/j.isci.2021.103468. eCollection 2021 Dec 17. iScience. 2021. PMID: 34888502 Free PMC article.

8

Genome-wide association and functional interrogation identified a variant at 3p26.1 modulating ovarian cancer survival among Chinese women.

Dai H, Chu X, Liang Q, Wang M, Li L, Zhou Y, Zheng Z, Wang W, Wang Z, Li H, Wang J, Zheng H, Zhao Y, Liu L, Yao H, Luo M, Wang Q, Kang S, Li Y, Wang K, Song F, Zhang R, Wu X, Cheng X, Zhang W, Wei Q, Li MJ, Chen K. Dai H, et al. Among authors: zheng z, zheng h. Cell Discov. 2021 Dec 21;7(1):121. doi: 10.1038/s41421-021-00342-6. Cell Discov. 2021. PMID: 34930913 Free PMC article.

9

An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping.

Wang Z, Liang Q, Qian X, Hu B, Zheng Z, Wang J, Hu Y, Bao Z, Zhao K, Zhou Y, Feng X, Yi X, Li J, Shi J, Liu Z, Hao J, Chen K, Yu Y, Sham PC, Lu W, Wang X, Song W, Li MJ. Wang Z, et al. Among authors: zheng z. Nat Commun. 2023 Mar 3;14(1):1208. doi: 10.1038/s41467-023-36897-z. Nat Commun. 2023. PMID: 36869052 Free PMC article.

10

Disruptor of telomeric silencing 1-like (DOT1L) is involved in breast cancer metastasis via transcriptional regulation of MALAT1 and ZEB2.

Duan Y, Zhang X, Yang L, Dong X, Zheng Z, Cheng Y, Chen H, Lan B, Li D, Zhou J, Xuan C. Duan Y, et al. Among authors: zheng z. J Genet Genomics. 2019 Dec 20;46(12):591-594. doi: 10.1016/j.jgg.2019.11.008. Epub 2019 Dec 17. J Genet Genomics. 2019. PMID: 31952940 No abstract available.

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